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Received: 14 February 2017 Revised: 14 July 2017 Accepted: 31 August 2017 DOI: 10.1002/ece3.3445
ORIGINAL RESEARCH
Ecotypic differences in the phenology of the tundra species Eriophorum vaginatum reflect sites of origin Thomas C. Parker1
| Jianwu Tang1
| Mahalia B. Clark1 | Michael M. Moody2 |
Ned Fetcher3 1 The Ecosystems Center, Marine Biological Laboratory, Woods Hole, MA, USA 2 Biological Sciences, University of Texas at El Paso, El Paso, TX, USA 3
Institute for Environmental Science and Sustainability, Wilkes University, Wilkes-Barre, PA, USA Correspondence Thomas C. Parker and Jianwu Tang, The Ecosystems Center, Marine Biological Laboratory, Woods Hole, MA, USA. Emails:
[email protected] (TCP) and
[email protected] (JT) Present Address Thomas C. Parker, Biological and Environmental Sciences, Faculty of Natural Sciences, University of Stirling, Stirling, UK Funding information National Science Foundation, Grant/Award Number: 1417645, 1417763 and 1418010
Abstract Eriophorum vaginatum is a tussock-forming sedge that contributes significantly to the structure and primary productivity of moist acidic tussock tundra. Locally adapted populations (ecotypes) have been identified across the geographical distribution of E. vaginatum; however, little is known about how their growth and phenology differ over the course of a growing season. The growing season is short in the Arctic and therefore exerts a strong selection pressure on tundra species. This raises the hypothesis that the phenology of arctic species may be poorly adapted if the timing and length of the growing season change. Mature E. vaginatum tussocks from across a latitudinal gradient (65–70°N) were transplanted into a common garden at a central location (Toolik Lake, 68°38′N, 149°36′W) where half were warmed using open-top chambers. Over two growing seasons (2015 and 2016), leaf length was measured weekly to track growth rates, timing of senescence, and biomass accumulation. Growth rates were similar across ecotypes and between years and were not affected by warming. However, southern populations accumulated significantly more biomass, largely because they started to senesce later. In 2016, peak biomass and senescence of most populations occurred later than in 2015, probably induced by colder weather at the beginning of the growing season in 2016, which caused a delayed start to growth. The finish was delayed as well. Differences in phenology between populations were largely retained between years, suggesting that the amount of time that these ecotypes grow has been selected by the length of the growing seasons at their respective home sites. As potential growing seasons lengthen, E. vaginatum may be unable to respond appropriately as a result of genetic control and may have reduced fitness in the rapidly warming Arctic tundra. KEYWORDS
Arctic tundra, common garden, ecotypes, Eriophorum vaginatum, growing season length, local adaptation, phenology, senescence
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. © 2017 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. Ecology and Evolution. 2017;1–12.
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1 | INTRODUCTION
Phenology, the timing of plant processes in relation to environmental cues, is a key control on productivity (Cleland, Chuine,
Climate change may force species into decline and eventual extinc-
Menzel, Mooney, & Schwartz, 2007) and could be sensitive to cli-
tion as local environmental conditions change and the geographical
mate change (Walther et al., 2002). The phenology of plants is
ranges of suitable growth conditions shift (Diffenbaugh & Field, 2013;
known to respond to temperature and photoperiod (Richardson
Thomas et al., 2004). The climate of the Arctic is warming at a faster
et al., 2012; Tang et al., 2016), but in high-latitude ecosystems
rate than the rest of the planet (Serreze & Barry, 2011) and may warm
24-hr days persist late into the growing season, meaning that plants
by up to 11°C by 2,100 should emissions of greenhouse gases fol-
may need other cues to trigger senescence including changes in light
low their current trajectories (IPCC 2013). Several arctic plant spe-
quality including the red:far-red light ratio (Nilsen, 1985) as well
cies show strong ecotypic differentiation across broad geographical
as temperature (Clapham, Ekberg, Eriksson, Norell, & Vince-Prue,
ranges due to local selection pressure; these may be slow to react to
2002; Clapham et al., 1998; Mølmann, Junttila, Johnsen, & Olsen,
climate change especially if there is limited gene flow between pop-
2006). Studies of plant phenology from temperate and boreal re-
ulations (Bennington et al., 2012; Chapin & Chapin, 1981; McGraw &
gions using common garden experiments have demonstrated that
Antonovics, 1983; McGraw et al., 2015). In recent years, arctic plants
plants from higher latitudes flower earlier (Olsson & Ågren, 2002;
have shown increases in growth and cover across many areas of the
Weber & Schmid, 1998). However, the opposite has been shown in
tundra (Elmendorf, Henry, Hollister, Bjork, Boulanger-Lapointe, et al.,
other study systems (Kalisz & Wardle, 1994). At present, ecotypic
2012); however, the response is not consistent across all plant func-
differentiation in plant phenology remains plausible but with limited
tional types (PFTs). This raises the question of whether climate change
evidence in the literature.
will offer opportunities to some PFTs while the response of others will be constrained by their recent evolutionary history.
In arctic ecosystems, plant growth is constrained by a very short growing season (Euskirchen et al., 2006). Furthermore, the seasonal
Eriophorum vaginatum L. (Cyperaceae) has demonstrated ecotypic
shifts from cold to warm and back again can occur extremely rapidly
differentiation across environmental gradients in the tundra and bo-
(Cherry et al., 2014). The length of the growing season at different
real ecosystems of Alaska (Shaver, Fetcher, & Chapin, 1986). E. vag-
sites could produce strong local selection for the timing of green-up
inatum is a tussock-forming sedge and a foundation species (Ellison
and senescence in arctic plants. Over recent decades, warmer tem-
et al., 2005) of moist acidic Arctic tundra, which contributes up to
peratures and smaller winter snowpacks have caused a significant
30% of annual primary productivity (Chapin & Shaver, 1985; Shaver,
lengthening of the potential growing season in arctic ecosystems, with
Bret-Harte, & Jones, 2001) and provides the characteristic tussock
both earlier thaw and later freeze-up (Euskirchen et al., 2006; Park
structure to moist acidic tundra (Chapin, van Cleve, & Chapin, 1979).
et al., 2016). However, snow removal and addition experiments to ma-
Populations of E. vaginatum have been shown to produce less biomass
nipulate the start of the growing season have shown that phenology
per tiller along a latitudinal gradient in Alaska from south to north
can be shifted, resulting in earlier green-up followed by earlier senes-
(Shaver et al., 1986). When populations are transplanted into com-
cence (Rosa et al., 2015; Semenchuk et al., 2016). In both of the cited
mon gardens north or south of their site of origin, they continue to
experiments, there was no net increase in growth period following the
show differences in leaf biomass production 3 years after being moved
earlier onset of growth, suggesting that there may be a genetic basis
(Fetcher & Shaver, 1990). After reciprocal transplanting, “home site
for duration of seasonal growth (Rosa et al., 2015). These results raise
advantage” is shown, whereby tussocks growing at the site of their
the question whether locally adapted arctic plants have the capacity
origin have fitness advantages in photosynthetic rates and biomass
to respond to longer growing seasons or whether other factors asso-
per leaf (Souther, Fetcher, Fowler, Shaver, & McGraw, 2014), new tiller
ciated with climate change (e.g., community change and stimulation of
production (McGraw et al., 2015), and ultimately survival (Bennington
growth [Elmendorf, Henry, Hollister, Bjork, Bjorkman, et al., 2012]) are
et al., 2012).
driving observed (Epstein et al., 2012) “greening” patterns.
Northern populations of E. vaginatum have particularly low produc-
Until now, growth rates and phenology of different ecotypes of
tivity when transplanted south into a warmer environment (Fetcher &
E. vaginatum have not been documented in detail through a growing
Shaver, 1990). On the other hand, shrubs in the genera Betula, Salix,
season. In this study, we measured growth rate of leaves, the date at
and Alnus have been observed to increase in growth rates and cover
which senescence started, and the date at which individuals reached
across the circumpolar region, primarily in response to increasing
their peak in greenness for six populations of E. vaginatum collected
summer temperatures and extended growing seasons (Elmendorf,
along a latitudinal gradient 4 years after transplanting into a common
Henry, Hollister, Bjork, Boulanger-Lapointe, et al., 2012; Myers-
garden. Specifically, we addressed the following questions: (1) Are
Smith et al., 2011). This is consistent with experiments which show
there ecotypic differences in growth rate and phenology that corre-
that shrub growth in the low Arctic often responds more positively
spond with previously observed differences in biomass accumulation
than sedges to warming using open-top chambers (OTCs) (Elmendorf,
(Shaver et al., 1986)? We hypothesized that ecotypes from further
Henry, Hollister, Bjork, Bjorkman, et al., 2012; Walker et al., 2006). If
south with warmer, longer growing seasons would grow faster and
E. vaginatum-dominated tundra were to shift to higher shrub coverage,
senesce later. (2) Can phenology and growth rates be influenced by
ecosystem processes will shift with changes in productivity and car-
experimental warming? Our second hypothesis was that these traits
bon turnover (Cahoon, Sullivan, Shaver, Welker, & Post, 2012).
would remain unaffected by warming because they have been under
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PARKER et al.
strong selection pressure and have limited capacity to respond to en-
described in Shaver and Laundre (1997). In each case, a small zip tie
vironmental change.
was secured around the base of the tiller, so as to include all leaves with any visible green portions, but to exclude any previously senesced
2 | MATERIALS AND METHODS 2.1 | Site description and experimental design A common garden with six different populations of the tussock- forming sedge, E. vaginatum, taken from different latitudes in Alaska
leaves from previous growth. The total leaf length and the length of the green portions were measured to the nearest 5 mm approximately once a week for each leaf in a tiller, from oldest to youngest.
2.3 | Environmental datasets
was established in moist acidic tussock tundra near Toolik Lake,
Data for cumulative thawing degree-days (TDD, defined as the sum
Alaska (68°38′N, 149°36′W), during summer 2011. Vegetation at
of the mean daily temperatures over 0°C), air temperature, and PAR
this site is dominated by tussocks of E. vaginatum, deciduous dwarf
in 2015 and 2016 were acquired from the meteorological stations
shrubs (Betula nana L. and Salix spp.) and evergreen shrubs (Vaccinium
operated by the Toolik Field Station Environmental Data Center
vitis-idaea L., Rhododendron tomentosum Harmanja [previously Ledum
of the University of Alaska, Fairbanks (Environmental Data Center
palustre], Cassiope tetragona L.) along with an understorey of mosses.
Team). Mean potential growing season length and mean annual TDD
The garden consisted of four replicate plots of plants from the six
for each of the six sites of origin were extracted and calculated from
different populations of E. vaginatum (three tussocks in each plot).
the SNOTEL database (http://www.wcc.nrcs.usda.gov/snow/). Here,
Tussocks were taken from three sites south of the Brooks Range and
growing season length was defined as the number of consecutive days
three sites north of the Range. The southern sites were Eagle Creek
of daily temperatures at or above 0°C.
(EC; 65°26′N, 145°31’W), No Name Creek (NN; 66°07′N, 150°10’W), and Coldfoot (CF; 67°15′N, 150°10’W) and the northern sites were Toolik Lake (TL; locally transplanted as a reference), Sagwon (SG; 69°25′N, 148°43’W), and Prudhoe Bay (PB; 70°20′N, 149°04’W).
2.4 | Data processing The study population consisted of 24 tillers, four each from six popu-
These six sites were used for previous long-term studies (Bennington
lations. The senesced portions of leaves were fragile and sometimes
et al., 2012; Shaver et al., 1986; Souther et al., 2014). Tussocks were
broke off; as this occurred after leaves had reached their full length,
transplanted in July 2011 according to the protocol of McGraw et al.
the total length was corrected to match the last measurement of the
(2015). A serrated knife was used to sever the rhizomes from roots
unbroken leaf. Where lengths of single leaves were missing for a time
and soil at a tussock’s base and remove it from the tundra. Tussocks
point due to human error, they were replaced with the mean of the pre-
from each site, including TL, were then placed in the vacant posi-
vious and following time points. Only leaves that were growing during
tions at the common garden where local tussocks had been removed.
the season of measurement were measured, thereby excluding leaves
This method has a high success rate due to E. vaginatum’s deciduous
that were grown in the previous year and were senescing as well as
rooting strategy; although roots are severed during transplanting,
leaves that had been initiated for the next year but were not elongating.
new roots grow in each subsequent year, restoring full root function
Growth rate was determined for these leaves for both years over similar
(Fetcher & Shaver, 1990; McGraw et al., 2015). Plots were arranged
time periods from mid-June until early August to permit comparisons
in pairs of the same population, and the spatial arrangement of these
between years. The date when senesced portions of actively growing
pairs was random. One of each of the pairs was randomly selected to
leaves were first observed was identified as the onset of senescence
be passively warmed using an OTC. The OTC has a cone shape with
for that tiller. In some cases, no senescence was observed and the last
a bottom diameter of 1.23 m and top diameter of 0.84 m and vertical
observation date in the dataset was used. We acknowledge that this
height 0.7 m, as modified from the OTCs used by the International
may be an underestimate of the date of actual senescence as defined
Tundra Experiment (ITEX) (Marion et al., 1997) by increasing the di-
above. The date at which the maximum green length of leaf was ob-
ameter and height (J. Tang, personal communication, 2011). The
served on the whole tiller was also determined. Maximum green length
OTCs were placed on the selected plots in 2015 from 11 July until 28
for each tiller was taken to be the maximum value of the summed green
August and in 2016 from 2 June until 28 August and caused a mean
leaf lengths of the whole tiller over the course of each growing season.
hourly air temperature increase of 1.16°C at 20 cm above the ground and an increase of 2.41°C when photosynthetically active radiation (PAR) was above 600 μmol m−2 s−1.
2.5 | Statistical analysis Linear mixed-effects models fitted with restricted maximum likelihood
2.2 | Leaf measurements Leaf growth and senescence were monitored from 17 June until 21
(REML) were used to analyze the effect of population, warming, and year as fixed effects on the response variables growth rate, senescence date, maximum green date, and maximum green length. Mixed-effects models
August in 2015 and from 2 June until 26 August in 2016. One tiller
were applied using the “nlme” package in R (Pinheiro, Bates, DebRoy, &
from the northernmost tussock of each plot was selected haphazardly
Sarkar, 2017; R Development Core Team 2016). The residuals of each
to monitor using tagging and measuring methods similar to those
model were normally distributed. Plot identity within the experiment
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PARKER et al.
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Air T (°C)
May
Max air T (°C)
Min air T (°C)
PAR (mol m−2 s−1)
2015
2016
2015
2016
2015
2016
2015
2016
4.6
0.8
10.4
5.7
−1.4
−4.4
449.8
451.4
June
9.0
6.6
14.0
11.5
3.3
−0.4
438.9
458.7
July
10.1
11.6
14.8
16.4
3.4
5.4
416.0
441.8
August
4.9
8.5
8.6
13.2
1.4
3.5
178.0
261.3
Average
7.1
6.9
11.9
11.7
1.7
1.0
370.7
403.3
T A B L E 1 Mean daily temperature and photosynthetically active radiation (PAR) data at Toolik Lake Field Station over the growing season in 2015 and 2016. In 2015 and 2016, winter snowpack melted on day 137 and 138, respectively (17 and 18 May)
T A B L E 2 Test statistics from linear mixed-effects models analyzing the effect of population, warming, and study year on four variables: growth rate, senescence starting date, date at which green leaves are at their maximum and the maximum green leaf length. Significant results (p .5*, p > .01**. Error bars represent ± 1 standard error of the mean. Abbreviations of site of origin names are provided below to aid interpretation. The number at each site abbreviation relates to the relative latitude of each site (1–6 from south to north)
Growth rate (cm/day)
1
(a)
(b)
0.8 0.6 0.4 0.2 6:PB
0 120
5:SG
130
140
4:TL
150
3:CF
1:EC 2:NN
160
170
6:PB
180
Home Growing Season length (Days)
600
5:SG 4:TL
800
1:EC 3:CF
2:NN
1,000 1,200 1,400 1,600 1,800 Home TDD
F I G U R E 2 Growth rates of green leaves of six populations of Eriophorum vaginatum in the common garden in relation to (a) growing season length or (b) thawing degree-days (TDD) of the site of origin of the population. Data from 2015 are represented by filled circles, and data from 2016 are represented by open circles. Correlation coefficients and lines are displayed if p .5*, p > .01**, p > .001***. Error bars represent ± 1 standard error of the mean. Abbreviations of site of origin names are provided below to aid interpretation. The number at each site abbreviation relates to the relative latitude of each site (1–6 from south to north) correlation was still present but with a less steep slope (0.62 reduced
of the six populations with only a small change in the TL plants and an
to 0.32). As in the case of senescence date, the y intercept of the
earlier start date in the EC plants in 2016 (Figure 5c). In 2016, the date
regression equation was higher than in 2015. Very similar patterns
of maximum green tissue occurred later than in 2015 in five of the six
were observed in 2015 and 2016 between home site TDD and the
populations, EC being the exception (Figure 5d).
date at which tillers reached their maximum green length (Figure 4b). Warming had no effect on either the start of senescence or the date at which maximum green length was reached on tillers (Table 2). More TDD were accumulated in 2015 than in 2016. By the end of the measurement period at Julian day 230, 881 TDD had accumulated in 2015 and 800 had accumulated in 2016 (Figure 5b). This was primarily due to a faster accumulation of TDD in the early season
4 | DISCUSSION 4.1 | Ecotypic differences in biomass accumulation but not growth rate Transplanted tussocks of E. vaginatum growing in a common garden
when temperatures were warmer than in 2016. After day 150, TDD
at Toolik Lake, Alaska showed clear differences in the length of the
increased in both years at similar rates. The mean starting date of se-
leaves that they produce. The trend over both measurement years
nescence was later in 2016 than in 2015 for four (PB, SG, CF, and NN)
was for southern populations, from sites with longer and warmer
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PARKER et al.
Air temperature (°C)
20
4.2 | Southern ecotypes grow later into the growing season
(a)
15 10 5
There was a positive relationship between the maximum length of
0
green leaves produced and both TDD and growing season length of
−5
the home site. This result was expected given that these were corre-
−10
lated with the higher productivity of E. vaginatum observed previously (Fetcher & Shaver, 1990). In both 2015 and 2016, southern ecotypes
−15 120
Cumulative TDD
800
140
160
180
200
220
240
season than northern ecotypes. With similar growth rates between
(b)
ecotypes, the southern ecotypes reached a higher peak biomass as a result of later onset of senescence.
600
In both years of this common garden study, ecotypes from sites
400
with a longer growing season senesced later in the season. This re2015 2016
200
Population
120
140
160
180
200
220
240
these ecotypic differences. The plants in the common garden came season can differ by up to 50 days. At northern sites such as Sagwon or Prudhoe Bay, the ability to grow late into the season would be se-
(c) Senescence start date
lected against because temperatures would be too low for growth and there would more likely be frost and snow cover late in the season. At southern sites, such as No Name Creek or Coldfoot, the growing sea120
PB SG TL CF NN EC
sult suggests a possible selection pressure that may have shaped from sites along a latitudinal gradient where the length of the growing
0
PB SG TL CF NN EC
of E. vaginatum reached peak green biomass later in the growing
140
160
180
200
220
240
son is longer and plants would have a competitive advantage if they senesced later.
(d) Max Green Date
These results are not consistent with other studies that examined ecotypic differentiation of phenology. For example, northern popu120
140
160
180
200
220
240
Day of the year
lations of three herbaceous species in temperate and boreal Europe (Lythrum salicaria, Solidago altissima, and Solidago gigantea) flowered earlier when grown in more southern common gardens (Olsson &
F I G U R E 5 Air temperature (a) and cumulative thawing degree- days (TDD) (b) in 2015 (solid line) and 2016 (dotted line) at Toolik Lake, AK compared with the mean senescence start date (c) and maximum green date (d) in either year (2015: closed circles, 2016: open circles) of different Eriophorum vaginatum populations at the same site. The arrows indicate the direction of change between 2015 and 2016 for each population
Ågren, 2002; Weber & Schmid, 1998). This could be the result of
growing seasons, to grow longer leaves. This is consistent with similar
Wardle, 1994). E. vaginatum lives much longer than the species men-
previous experiments in this system, both at Toolik Lake and at other
tioned above (Mark, Fetcher, Shaver, & Chapin, 1985), and thus, its
transplant gardens along the latitudinal gradient in Alaska (Fetcher &
phenology may be subject to different selection pressures.
selection for immediate response to spring temperature increases. The opposite was observed in populations of the North American herb Campanula americana; populations from Florida, Georgia, and Kentucky flowered earlier than those from further north in Michigan (Kalisz & Wardle, 1994). This result was attributed to the greater abundance of biennial morphs of the species in northern states (Kalisz &
Shaver, 1990; Shaver et al., 1986; Souther et al., 2014). The prevailing
The hypothesis that ecotypic differences in senescence timing
hypothesis to explain these observed differences is that the milder
may be controlled by an adaptation to growing season length is sup-
growing conditions in southern sites have selected for more produc-
ported by experimental evidence from Toolik Lake. Rosa et al. (2015)
tive phenotypes which continue to be expressed even 30 years after
showed that if the growing season is artificially brought forward by
transplanting (Souther et al., 2014). The present study tracked leaf
removing snow in May, the buds of seven of eight dominant tundra
growth of E. vaginatum over a growing season and helps to explain the
plant species, including E. vaginatum, will break earlier, but also se-
differences between ecotypes that have been observed in previous
nesce earlier. As a result, there was no increase in growing period,
studies. We hypothesized that southern ecotypes would have higher
suggesting that annual growth time is under genetic control shaped
growth rates. However, the present study does not support this idea.
by selection pressure (Rosa et al., 2015). Another experimental early-
Although there was high variability in the data, there were no signifi-
season increase in snow in the high Arctic (Svalbard) produced a sim-
cant differences in growth rate between ecotypes. These data there-
ilar effect whereby late onset of growth results in late senescence for
fore lead us to suggest an alternative (but not exclusive) hypothesis
all species studied (Semenchuk et al., 2016). As with Rosa et al. (2015),
that the length of the growing season at the home site produces more
the change in the timing of phenology had no effect on the period
biomass accumulation.
of active growth, suggesting a genetic control over the window for
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PARKER et al.
8
growth in arctic plants (Semenchuk et al., 2016). Consequently, the
increases the cover of graminoids as well as shrubs, but the effect is
present study and previous work may have important implications for
more variable and less definitive (Elmendorf, Henry, Hollister, Bjork,
future vegetation dynamics under climate change. Potential growing
Bjorkman, et al., 2012). In fact, long-term monitoring of control plots
seasons are getting longer in the Arctic as a result of both earlier melt
in the ITEX has also observed increases in deciduous shrub cover
of the winter snowpack and later freeze-up (Euskirchen et al., 2006;
in comparison with sedges which have shown, on average, very lit-
Park et al., 2016). Growth of short-season plants may start earlier, but
tle change (Elmendorf, Henry, Hollister, Bjork, Boulanger-Lapointe,
under genetic constraints they will senesce earlier despite favorable
et al., 2012). With this in mind, it is becoming clearer that prominent
growing conditions in the late season. To better understand how ge-
graminoid species such as E. vaginatum may be at a competitive disad-
netic constraints will feed into interspecific competitive interactions,
vantage in relation to faster-growing species with growth strategies
common garden studies of phenology need to be performed for dif-
that can respond more quickly to more benign growing conditions
ferent tundra PFTs. We hypothesize that groups such as deciduous
(Bret-Harte et al., 2001).
shrubs can extend their window of growth in response to longer grow-
The experiments mentioned in the previous paragraph used pop-
ing seasons because they have shown to be phenotypically plastic
ulations of graminoids from north of the tree line. They support the
(Bret-Harte et al., 2001) in some traits, but this still needs to be tested
hypothesis that graminoids, including E. vaginatum, are likely to be
regarding phenology.
outcompeted by deciduous shrubs in a warming climate, although the results of competition may not become evident until 10 years or more
4.3 | Leaf growth and phenology not responsive to experimental warming
have passed (Elmendorf, Henry, Hollister, Bjork, Boulanger-Lapointe, et al., 2012). With the exception of the present study, no warming experiments have used graminoid populations from south of the tree
Neither leaf growth rate nor timing of senescence responded to ex-
line. Thus, it is difficult to predict how the populations of E. vagina-
perimental warming. This supports our hypothesis that E. vaginatum
tum from south of the tree line will respond to climate warming, al-
ecotypes have been shaped by strong selection pressures and have
though they are apparently able to maintain themselves for more than
a very limited capacity to respond to changes in environmental con-
100 years under conditions that prevailed prior to the early 1980s
ditions. A previous warming experiment at Toolik Lake observed in-
(Mark et al., 1985). It is possible that gene flow from the south may be
creased leaf production of E. vaginatum in response to warming (using
able to produce a phenotype that is better able to compete with the
a similar method) but only in the early season, after which no differ-
shrubs, although it is not clear whether it will be able to keep up with
ence in growth rate was observed between warmed and control plants
the projected rate of warming (McGraw et al., 2015).
(Sullivan & Welker, 2005). It is therefore possible that we would have seen differences between treatments if warming was applied earlier in the season (mid-May). Other warming experiments have resulted in no increase in photosynthetic rate of E. vaginatum (Starr, Oberbauer,
4.4 | Phenology is more responsive to interannual climate variation than in situ warming
& Ahlquist, 2008), no increase in growth rate (Natali, Schuur, & Rubin,
While there were differences in the timing of senescence between
2012), or negligible effects on vegetative growth in graminoids (Arft
ecotypes, there was no significant effect of warming on timing
et al., 1999). We conclude that differences between ecotypes ob-
of senescence, a finding that concurs with other warming studies
served by Fetcher and Shaver (1990) are not due to differences in
(Bjorkman, Vellend, Frei, & Henry, 2017; Rosa et al., 2015) as well as
growth rate. Thus, no specific ecotype will have a selective advantage
long-term datasets which show that phenology of arctic plants is rela-
under climate change due to growth rate.
tively unresponsive to recent climate change (Oberbauer et al., 2013).
The finding that the growth rate of leaves of E. vaginatum does
A long-term warming experiment also found that phenology of high
not respond to warming is relevant in light of a rapidly changing arc-
arctic plants was not responsive to warming, but year-to-year vari-
tic climate and the increased dominance of likely more competitive
ation in phenology could be explained by snowmelt date (Bjorkman,
plants (Myers-Smith et al., 2011). There is still uncertainty surround-
Elmendorf, Beamish, Vellend, & Henry, 2015). Temperatures are
ing the relative response of different PFTs to future climate change
warming in arctic ecosystems at unprecedented rates (Serreze &
(Elmendorf, Henry, Hollister, Bjork, Bjorkman, et al., 2012), especially
Barry, 2011), but our data suggest that warming within the range of
that of phenology (Oberbauer et al., 2013); however, evidence thus
our OTC treatment (2.4°C on sunny days) may not delay the onset
far would imply that deciduous shrubs that are already present in the
of senescence even if conditions are still conducive for continued
tundra represent the most negative future competitive interaction to
photosynthesis.
E. vaginatum. Common tundra shrubs such as Betula nana have been
In the present study, plants from four of the populations showed
shown to exhibit developmental plasticity (e.g., increased branching,
the first signs of senescence later in 2016 than in 2015. Similarly, the
canopy density) in response to release from abiotic stress (Bret-Harte
date at which maximum green leaf length was observed (which inte-
et al., 2001). Warming experiments with open-top chambers and
grates across leaves on a tiller) was later for five of the populations.
greenhouses cause an increase in canopy height and cover of de-
The difference in phenology coincides with differences in abiotic
ciduous shrubs in the low Arctic (Elmendorf, Henry, Hollister, Bjork,
conditions between 2015 and 2016. Melt of the winter snowpack oc-
Bjorkman, et al., 2012; Walker et al., 2006). Experimental warming
curred at approximately the same time in both years, but after this
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9
PARKER et al.
the 2 years diverged substantially. Other work has shown that that
1983). Thus, while there is support for endogenous rhythms in E. vagi-
timing of snowmelt influences phenological stages (Bjorkman et al.,
natum, there are other factors that can affect growing period.
2015; Rosa et al., 2015; Semenchuk et al., 2016), but on an annual
Ecotypes are also potentially responding to environmental cues
basis, photoperiod and warmer temperatures are the best predictors
that could, in part, be driving the adaptive endogenous rhythm. As
of bud break (Rosa et al., 2015). In the present study, the snow melted
senescence and maximum green day increase with decreasing lati-
at a similar time, but temperatures stayed lower later in 2016 com-
tude of the site of origin, both photoperiod and temperature could be
pared to 2015. With the assumption that all the ecotypes initiated
cues, and have been identified as consistent predictors of senescence
growth at the same time and that length of growing season remains
in the arctic flora (Rosa et al., 2015). Photoperiod and light quality
consistent (Rosa et al., 2015), the later senescence and peak biomass
are closely associated and predicable on an annual basis. However,
in 2016 suggest that the growing season started later. In this case,
photoperiod at high latitudes is poorly defined due to the 24-hr day-
the alleviation of cold temperatures may be the cue for growth initi-
light. At Toolik Lake, the sun remains above the horizon from day of
ation. The current understanding of the start of the growing season
the year 140 (May 20) through day 204 (July 23), which comprises
and subsequent phenological phases is that the timing of snowmelt is
most of the growing season and includes the period when senes-
important (Bjorkman et al., 2015; Rosa et al., 2015), but temperature
cence of the northern populations is initiated (Figure 1). At Tromsø,
has a significant predictive role (Rosa et al., 2015); therefore, air tem-
Norway (69°39′N), which is only slightly farther north than Toolik
perature succeeding snowmelt merits further study.
Lake, photoperiod undergoes a short period of rapid lengthening in
It is notable that the clinal difference between ecotypes was re-
mid-May followed by a period of no change once the sun is above the
duced in 2016 and 2015. This could simply be due to interannual vari-
horizon for 24 hr (Nilsen, 1985). In late July, there is a corresponding
ation which may have a disproportionate effect on the patterns that
period of rapid shortening followed by a period of gradual shortening
we observed due to the low sample size in this experiment or it could
(Nilsen, 1985). Because the pattern of rapid lengthening and short-
reflect a number of other factors that relate to the biology of E. vagi-
ening of the photoperiod varies greatly with small changes in latitude
natum. They could be exhibiting a slow acclimation to the new site at
(Nilsen, 1985), it could serve as a phenological cue for plant popula-
Toolik; however, the plants had already been in place for 4 years in
tions native to high latitudes.
2015 and transplants continue to exhibit ecotypic differentiation up
Another related cue that varies less drastically than photoperiod is
to 30 years after transplanting (Souther et al., 2014). Alternatively, the
light quality that could be measured by the ratio (R:FR) of red (660 nm)
growth and senescence of tillers could be influenced by environmen-
to far-red (730 nm) light (Mølmann et al., 2006; Nilsen, 1985). As the
tal conditions and metabolism from the previous year. New leaves of
sun drops below 10° above the horizon, red light is absorbed by the
E. vaginatum are set the year prior to their growth (Shaver & Laundre,
atmosphere and the R:FR ratio decreases. At Tromsø during the sum-
1997), and some of the patterns that we observe in their growth may
mer solstice, R:FR drops from 1.05 to 0.9 at midnight (Nilsen, 1985).
be influenced by factors such as carbohydrate storage from the pre-
Farther south at 60°N, it drops to 0.65 because the sun goes below the
vious growing season (Chapin, Shaver, & Kedrowski, 1986). It is clear
horizon, and farther north at 78°N, it hardly changes because the sun
that a longer record of the growth patterns of these ecotypes in a
is above the horizon. R:FR ratio has been shown to affect the balance
common garden will be required in order to elucidate all of the drivers
between the active and inactive forms of phytochrome (Leyser & Day,
of patterns that we observe.
2015), which is in turn responsible for germination and flowering as well as morphological changes in response to shading. Phytochrome
4.5 | Phenological cues in arctic ecosystems
seems to perform the same functions in the Cyperaceae as in other families. Kettenring, Gardner, and Galatowitsch (2006) found that
The differences in the timing of the onset of senescence and maximum
germination of wetland Carex sp. (Cyperaceace) was inducible and
green date between ecotypes suggest that each has its endogenous
reversible by alternating applications of red and far-red light, which
rhythm of growth and senescence or that the ecotypes were respond-
strongly suggests activity of phytochrome. Fetcher (1985) found in-
ing differently to an environmental cue. The endogenous rhythm hy-
creased tillering in response to a likely change in light quality follow-
pothesis is supported by phenological studies in the Arctic, which show
ing the removal of shrubs and mosses from tussocks of E. vaginatum
that snowmelt timing is a predictor of senescence across a range of
(with no concurrent change in nutrients with treatment). R:FR would
PFTs (Bjorkman et al., 2015; Rosa et al., 2015; Semenchuk et al., 2016).
also be clearly linked to the timing of the onset of winter which would
Under this hypothesis, once growth is initiated, it proceeds for a fixed
be dramatically different on the far ends of the latitudinal gradient of
number of days until senescence is initiated. For E. vaginatum ecotypes,
the ecotypes; thus, R:FR should be a consistent predictor of seasonal
this rhythm would be adaptive for variance across the latitudinal gradi-
change. We propose that as the ecotypes are from different latitudes,
ent from which each originates, likely based on environmental condi-
they differ in their sensitivity to R:FR changes. In this case, ecotypes
tions. This is supported by our data which suggests senescence and
from north of Toolik Lake (SG and PB) are more sensitive to R:FR light
maximum green date are closely linked to TDD and growing season
change and senesce earliest. Southern ecotypes would require a more
length. However, unusual events such as a period of below normal
pronounced R:FR reduction to initiate senescence, hence senescing
temperatures (in 1981 at Eagle Creek, AK) can lead to premature se-
later when in a common garden. If this annual rhythm is a genetic
nescence of the majority of a community (McGraw, Chester, & Stuart,
constraint, it could have repercussions for the long-term fitness of
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PARKER et al.
10
E. vaginatum, especially if southern ecotypes have a limited capacity for gene flow north, where they would have a better ability to take advantage of the longer potential growing seasons.
5 | CONCLUSIONS The phenology of E. vaginatum ecotypes grown in a common garden shows that differences in biomass observed in previous transplant experiments are in part due to southern ecotypes growing later into the season, not that they have a higher growth rate than northern ecotypes. The data suggest that the difference in timing of senescence could be caused by local adaptations whereby ecotypes grow for different amounts of time, depending on the length of the growing season at their home site. The comparison of phenology over two contrasting growing seasons shows that the timing of senescence is responsive from year to year to abiotic conditions. When conditions were suitable to start growth earlier in the year, most ecotypes in this study reached their peak biomass and started to senesce earlier. Therefore, differences in phenology between ecotypes were retained over the 2 years. These results have implications for the future fitness of E. vaginatum with rapid climate change (IPCC 2013) along with lengthening of the growing season (Park et al., 2016). If the length of time that E. vaginatum grows in any given season does not vary, these locally adapted ecotypes may not be able to take advantage of longer, warmer summers if spring also starts early. In this scenario, E. vaginatum would suffer adaptive lag (McGraw et al., 2015), while other species such as shrubs, which may hold a competitive advantage in a warming Arctic (Elmendorf, Henry, Hollister, Bjork, Bjorkman, et al., 2012), would accelerate the community change that is already being observed in arctic landscapes (Myers-Smith et al., 2011).
ACKNOWLE DG ME NTS The study was primarily funded by NSF/PLR 1418010 (to NF), NSF/ PLR 1417763 (to JT), and NSF/PLR 1417645 (to MM). We acknowledge the logistic support from the Toolik Station managed by the University of Alaska, Fairbanks, and the Arctic LTER project. Many thanks to Steven Unger, Darrel Dech, Stephen Turner, Stephen Forney, Mayra Melendez, Alana Thurston, and Elizabeth Fortin for field assistance and to Gaius Shaver for constructive comments on the manuscript. The authors have no conflict of interests.
AUTHORS’ CONTRI BUTI O N S NF, JT, and MM set up the experiment. TP and MC collected and analyzed the data. TP, NF, MM, and JT wrote the manuscript.
O RCI D Thomas C. Parker Jianwu Tang
http://orcid.org/0000-0002-3648-5316
http://orcid.org/0000-0003-2498-9012
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How to cite this article: Parker TC, Tang J, Clark MB, Moody MM, Fetcher N. Ecotypic differences in the phenology of the tundra species Eriophorum vaginatum reflect sites of origin.
SUPPORTI NG I NFO RM ATI O N Additional Supporting Information may be found online in the supporting information tab for this article.
Ecol Evol. 2017;00:1–12. https://doi.org/10.1002/ece3.3445